Clinical Research Coordinator II Job Dallas area,Texas USA,Healthcare

WHY UT SOUTHWESTERN?

With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals.

Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!

WHY UT SOUTHWESTERN?

Job Summary

Works under the direction of an Investigator(s) with limited supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.

Support Matthew Johnson, DPM, on clinical wound healing podiatry research in a 2-year appointment.

Perform research protocol tasks, review and abstract information from medical records, enter data into data collection forms and systems, perform data queries and edits, compile data for regulatory requirements, maintain databases and ensure data integrity, perform QA/QC clinical analyses, data checks, and error correction, prepare submissions to the IRB, performance sites, CTCA, and Clinical Trials.gov, assist with and prepare research records for audits, recruit and enroll patients in research studies, conduct and document informed consent for participants, maintain research supplies, assist with specimen collection and processing, assist in preparing studies for closeout, perform study procedures such as phlebotomy, vital signs, EKGs, wound imaging, and other procedures needed for research studies, may perform basic patient care skills under the direction of the PI, assist the PI with fiscal management of clinical trials, including budget preparation, and assist with research billing activities.

Benefits

PPO medical plan, available day one at no cost for full-time employee-only coverage
100% coverage for preventive healthcare-no copay
Paid Time Off, available day one
Retirement Programs through the Teacher Retirement System of Texas (TRS)
Paid Parental Leave Benefit
Wellness programs
Tuition Reimbursement
Public Service Loan Forgiveness (PSLF) Qualified Employer
Learn more about these and other UTSW employee benefits!

Required EXPERIENCE AND EDUCATION

Education Bachelor's Degree in medical or science related field
Experience 2 years years clinical research experience. May consider additional years of experience or advanced degree in lieu of education or experience, respectively.

Preferred

Licenses and Certifications (BLS) BASIC LIFE SUPPORT may be required based on research study protocols or affiliate location requirements. (CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements. ACRP or SOCRA certification a plus.

Job Duties

Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Interacts via telephone, telehealth or in-person.
Coordinates regulatory documentation for research studies that includes maintaining information to comply with industry standards, University policies, FDA requirements or other hospital policies.
Coordinates and schedules procedures as per research study. A…